510(k) K831921
K831921 is an FDA 510(k) premarket notification submitted by Polymer Technology Corp. for the device "DISPOSABLE MICROTOME BLADES". The FDA issued a decision of Substantially Equivalent on July 29, 1983. The device falls under product code IDL (Microtome, Accessories), a Class I device regulated under 21 CFR 864.3010. Polymer Technology Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 1983
- Date Received
- June 14, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Microtome, Accessories
- Device Class
- Class I
- Regulation Number
- 864.3010
- Review Panel
- PA
- Submission Type